NDC 82338-438 Benjamins Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82338-438
Proprietary Name:
Benjamins Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
P. A Benjamin Manufacturing Co Ltd
Labeler Code:
82338
Start Marketing Date: [9]
12-31-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333 - LIGHT BLUE)

Product Packages

NDC Code 82338-438-24

Package Description: 240 mL in 1 BOTTLE, PUMP

NDC Code 82338-438-38

Package Description: 3800 mL in 1 BOTTLE, PLASTIC

NDC Code 82338-438-60

Package Description: 60 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 82338-438?

The NDC code 82338-438 is assigned by the FDA to the product Benjamins Hand Sanitizer which is product labeled by P. A Benjamin Manufacturing Co Ltd. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 82338-438-24 240 ml in 1 bottle, pump , 82338-438-38 3800 ml in 1 bottle, plastic , 82338-438-60 60 ml in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Benjamins Hand Sanitizer?

Place enough product in the palms to thoroughly cover hands. Rub hands together briskly until dry. Do not rinse. Children under 6 years of age should be supervised by an adult.

Which are Benjamins Hand Sanitizer UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Benjamins Hand Sanitizer Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".